Canonical Allele Identifier: CA395733127

Gene: ARMC5

Linked Data

• gnomAD v4: 16-31462496-G-T
• MyVariant Identifiers: chr16:g.31473817G>T (hg19) ; chr16:g.31462496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462496G>T , CM000678.2:g.31462496G>T	GRCh38
NC_000016.9:g.31473817G>T , CM000678.1:g.31473817G>T	GRCh37
NC_000016.8:g.31381318G>T	NCBI36
NG_034258.1:g.9224G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.949G>T MANE Select	ENSP00000268314.4:p.Ala317Ser
ENST00000268314.8:c.949G>T	ENSP00000268314.4:p.Ala317Ser
ENST00000408912.7:c.1234G>T	ENSP00000386125.3:p.Ala412Ser
ENST00000457010.6:c.949G>T	ENSP00000399561.2:p.Ala317Ser
ENST00000538189.5:c.457G>T	ENSP00000443995.2:p.Ala153Ser
ENST00000563544.5:c.949G>T	ENSP00000456877.1:p.Ala317Ser
ENST00000564900.1:c.213-276G>T
NM_001105247.1:c.949G>T	NP_001098717.1:p.Ala317Ser
NM_001288767.1:c.1234G>T	NP_001275696.1:p.Ala412Ser
NM_001301820.1:c.1045G>T	NP_001288749.1:p.Ala349Ser
NM_024742.2:c.949G>T	NP_079018.1:p.Ala317Ser
XM_006721091.1:c.1045G>T	XP_006721154.1:p.Ala349Ser
XM_006721091.3:c.1045G>T	XP_006721154.1:p.Ala349Ser
XM_024450448.1:c.1045G>T	XP_024306216.1:p.Ala349Ser
XM_024450449.1:c.1045G>T	XP_024306217.1:p.Ala349Ser
NM_001105247.2:c.949G>T MANE Select	NP_001098717.1:p.Ala317Ser
NM_001288767.2:c.1234G>T	NP_001275696.1:p.Ala412Ser