Canonical Allele Identifier: CA366255150

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535946A>G (hg19) ; chr6:g.158114914A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114914A>G , CM000668.2:g.158114914A>G	GRCh38
NC_000006.11:g.158535946A>G , CM000668.1:g.158535946A>G	GRCh37
NC_000006.10:g.158455934A>G	NCBI36
NG_032889.1:g.58367T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.771T>C	ENSP00000391168.2:n.771T>C
ENST00000607071.6:c.*1279T>C	ENSP00000475855.1:n.*1279T>C
ENST00000642244.1:c.1469T>C	ENSP00000493554.1:p.Val490Ala
ENST00000642903.1:c.1559T>C	ENSP00000493559.1:p.Val520Ala
ENST00000644972.1:c.1559T>C	ENSP00000496451.1:p.Val520Ala
ENST00000645077.1:c.*1180T>C	ENSP00000496113.1:n.*1180T>C
ENST00000645172.1:c.*1261T>C	ENSP00000495367.1:n.*1261T>C
ENST00000646190.1:n.2890T>C
ENST00000646208.1:c.1295T>C	ENSP00000493723.1:p.Val432Ala
ENST00000646410.1:c.1430T>C	ENSP00000494205.1:p.Val477Ala
ENST00000646562.1:c.*1393T>C	ENSP00000496087.1:n.*1393T>C
ENST00000647468.2:c.1559T>C MANE Select	ENSP00000496731.1:p.Val520Ala
ENST00000648111.1:c.*1247T>C	ENSP00000497275.1:n.*1247T>C
ENST00000367101.5:c.*7T>C	ENSP00000356068.1:n.*7T>C
ENST00000367104.7:c.1559T>C	ENSP00000356071.3:p.Val520Ala
ENST00000435180.5:c.284T>C	ENSP00000391168.1:p.Val95Ala
ENST00000606965.5:c.*120T>C	ENSP00000475808.1:n.*120T>C
ENST00000607071.5:c.*1493T>C	ENSP00000475855.1:n.*1493T>C
ENST00000607742.5:c.*2837T>C	ENSP00000475523.1:n.*2837T>C
NM_032861.3:c.1559T>C	NP_116250.3:p.Val520Ala
NR_073096.1:n.1492T>C
XM_006715586.1:c.1349T>C	XP_006715649.1:p.Val450Ala
XM_011536196.1:c.1538T>C	XP_011534498.1:p.Val513Ala
XM_011536197.1:c.1445T>C	XP_011534499.1:p.Val482Ala
XM_011536198.1:c.1349T>C	XP_011534500.1:p.Val450Ala
XM_006715586.3:c.1349T>C	XP_006715649.1:p.Val450Ala
XM_011536196.3:c.1538T>C	XP_011534498.1:p.Val513Ala
XM_011536198.3:c.1349T>C	XP_011534500.1:p.Val450Ala
XM_024446573.1:c.1559T>C	XP_024302341.1:p.Val520Ala
XR_001743697.2:n.1590T>C
XR_942606.2:n.1641T>C
NM_032861.4:c.1559T>C MANE Select	NP_116250.3:p.Val520Ala
NR_073096.2:n.1474T>C