Canonical Allele Identifier: CA342652012

Gene: MUC1

Linked Data

• dbSNP Id: rs4072037
• gnomAD v4: 1-155192276-C-G
• MyVariant Identifiers: chr1:g.155162067C>G (hg19) ; chr1:g.155192276C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155192276C>G , CM000663.2:g.155192276C>G	GRCh38
NC_000001.10:g.155162067C>G , CM000663.1:g.155162067C>G	GRCh37
NC_000001.9:g.153428691C>G	NCBI36
NG_029383.1:g.5640G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000337604.6:c.66G>C	ENSP00000338983.5:p.Thr22=
ENST00000338684.9:c.93G>C	ENSP00000343482.6:p.Thr31=
ENST00000342482.8:c.93G>C	ENSP00000342814.4:p.Thr31=
ENST00000343256.9:c.66G>C	ENSP00000339690.5:p.Thr22=
ENST00000368389.6:c.66G>C	ENSP00000357374.2:p.Thr22=
ENST00000368390.7:c.66G>C	ENSP00000357375.3:p.Thr22=
ENST00000368392.7:c.93G>C	ENSP00000357377.3:p.Thr31=
ENST00000368393.7:c.66G>C	ENSP00000357378.3:p.Thr22=
ENST00000368396.8:c.93G>C	ENSP00000357381.4:p.Thr31=
ENST00000368398.7:c.66G>C	ENSP00000357383.3:p.Thr22=
ENST00000438413.5:c.66G>C	ENSP00000389098.1:p.Thr22=
ENST00000457295.6:c.93G>C	ENSP00000388172.3:p.Thr31=
ENST00000462215.5:c.93G>C	ENSP00000480335.1:p.Thr31=
ENST00000466913.1:n.132-29G>C
ENST00000467134.5:c.93G>C	ENSP00000484006.1:p.Thr31=
ENST00000471283.5:c.66G>C	ENSP00000484730.1:p.Thr22=
ENST00000498431.5:c.66G>C	ENSP00000483128.1:p.Thr22=
ENST00000610359.4:c.93G>C	ENSP00000483482.1:p.Thr31=
ENST00000610468.4:c.66G>C	ENSP00000482688.1:p.Thr22=
ENST00000611571.4:c.66G>C	ENSP00000480333.1:p.Thr22=
ENST00000611577.4:c.59-2G>C	ENSP00000483581.1:n.59-2G>C
ENST00000612778.4:c.93G>C	ENSP00000484824.1:p.Thr31=
ENST00000614519.4:c.93G>C	ENSP00000482988.1:p.Thr31=
ENST00000615517.4:c.93G>C	ENSP00000483473.1:p.Thr31=
ENST00000620103.4:c.66G>C	ENSP00000481231.1:p.Thr22=
ENST00000620770.1:n.159G>C
NM_001018016.2:c.93G>C	NP_001018016.1:p.Thr31=
NM_001018017.2:c.66G>C	NP_001018017.1:p.Thr22=
NM_001044390.2:c.66G>C	NP_001037855.1:p.Thr22=
NM_001044391.2:c.66G>C	NP_001037856.1:p.Thr22=
NM_001044392.2:c.93G>C	NP_001037857.1:p.Thr31=
NM_001044393.2:c.66G>C	NP_001037858.1:p.Thr22=
NM_001204285.1:c.66G>C	NP_001191214.1:p.Thr22=
NM_001204286.1:c.93G>C	NP_001191215.1:p.Thr31=
NM_001204287.1:c.93G>C	NP_001191216.1:p.Thr31=
NM_001204288.1:c.93G>C	NP_001191217.1:p.Thr31=
NM_001204289.1:c.93G>C	NP_001191218.1:p.Thr31=
NM_001204290.1:c.59-29G>C	NP_001191219.1:n.59-29G>C
NM_001204291.1:c.93G>C	NP_001191220.1:p.Thr31=
NM_001204292.1:c.93G>C	NP_001191221.1:p.Thr31=
NM_001204293.1:c.66G>C	NP_001191222.1:p.Thr22=
NM_001204294.1:c.66G>C	NP_001191223.1:p.Thr22=
NM_001204295.1:c.93G>C	NP_001191224.1:p.Thr31=
NM_001204296.1:c.93G>C	NP_001191225.1:p.Thr31=
NM_001204297.1:c.93G>C	NP_001191226.1:p.Thr31=
NM_002456.5:c.66G>C	NP_002447.4:p.Thr22=
NM_001018016.3:c.93G>C	NP_001018016.1:p.Thr31=
NM_001018017.3:c.66G>C	NP_001018017.1:p.Thr22=
NM_001044390.3:c.66G>C	NP_001037855.1:p.Thr22=
NM_001044391.3:c.66G>C	NP_001037856.1:p.Thr22=
NM_001044392.3:c.93G>C	NP_001037857.1:p.Thr31=
NM_001044393.3:c.66G>C	NP_001037858.1:p.Thr22=
NM_001204285.2:c.66G>C	NP_001191214.1:p.Thr22=
NM_001204287.2:c.93G>C	NP_001191216.1:p.Thr31=
NM_001204288.2:c.93G>C	NP_001191217.1:p.Thr31=
NM_001204289.2:c.93G>C	NP_001191218.1:p.Thr31=
NM_001204290.2:c.59-29G>C	NP_001191219.1:n.59-29G>C
NM_001204293.2:c.66G>C	NP_001191222.1:p.Thr22=
NM_001204294.2:c.66G>C	NP_001191223.1:p.Thr22=
NM_001204296.2:c.93G>C	NP_001191225.1:p.Thr31=
NM_001204297.2:c.93G>C	NP_001191226.1:p.Thr31=
NM_001371720.1:c.93G>C	NP_001358649.1:p.Thr31=
NM_002456.6:c.66G>C	NP_002447.4:p.Thr22=