Canonical Allele Identifier: CA366255226

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535974C>A (hg19) ; chr6:g.158114942C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114942C>A , CM000668.2:g.158114942C>A	GRCh38
NC_000006.11:g.158535974C>A , CM000668.1:g.158535974C>A	GRCh37
NC_000006.10:g.158455962C>A	NCBI36
NG_032889.1:g.58339G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.743G>T	ENSP00000391168.2:n.743G>T
ENST00000607071.6:c.*1251G>T	ENSP00000475855.1:n.*1251G>T
ENST00000642244.1:c.1441G>T	ENSP00000493554.1:p.Ala481Ser
ENST00000642903.1:c.1531G>T	ENSP00000493559.1:p.Ala511Ser
ENST00000644972.1:c.1531G>T	ENSP00000496451.1:p.Ala511Ser
ENST00000645077.1:c.*1152G>T	ENSP00000496113.1:n.*1152G>T
ENST00000645172.1:c.*1233G>T	ENSP00000495367.1:n.*1233G>T
ENST00000646190.1:n.2862G>T
ENST00000646208.1:c.1267G>T	ENSP00000493723.1:p.Ala423Ser
ENST00000646410.1:c.1402G>T	ENSP00000494205.1:p.Ala468Ser
ENST00000646562.1:c.*1365G>T	ENSP00000496087.1:n.*1365G>T
ENST00000647468.2:c.1531G>T MANE Select	ENSP00000496731.1:p.Ala511Ser
ENST00000648111.1:c.*1219G>T	ENSP00000497275.1:n.*1219G>T
ENST00000367101.5:c.1575G>T	ENSP00000356068.1:p.Lys525Asn
ENST00000367104.7:c.1531G>T	ENSP00000356071.3:p.Ala511Ser
ENST00000435180.5:c.256G>T	ENSP00000391168.1:p.Ala86Ser
ENST00000606965.5:c.*92G>T	ENSP00000475808.1:n.*92G>T
ENST00000607071.5:c.*1465G>T	ENSP00000475855.1:n.*1465G>T
ENST00000607742.5:c.*2809G>T	ENSP00000475523.1:n.*2809G>T
NM_032861.3:c.1531G>T	NP_116250.3:p.Ala511Ser
NR_073096.1:n.1464G>T
XM_006715586.1:c.1321G>T	XP_006715649.1:p.Ala441Ser
XM_011536196.1:c.1510G>T	XP_011534498.1:p.Ala504Ser
XM_011536197.1:c.1417G>T	XP_011534499.1:p.Ala473Ser
XM_011536198.1:c.1321G>T	XP_011534500.1:p.Ala441Ser
XM_006715586.3:c.1321G>T	XP_006715649.1:p.Ala441Ser
XM_011536196.3:c.1510G>T	XP_011534498.1:p.Ala504Ser
XM_011536198.3:c.1321G>T	XP_011534500.1:p.Ala441Ser
XM_024446573.1:c.1531G>T	XP_024302341.1:p.Ala511Ser
XR_001743697.2:n.1562G>T
XR_942606.2:n.1613G>T
NM_032861.4:c.1531G>T MANE Select	NP_116250.3:p.Ala511Ser
NR_073096.2:n.1446G>T