Canonical Allele Identifier: CA366254962

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535859A>G (hg19) ; chr6:g.158114827A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114827A>G , CM000668.2:g.158114827A>G	GRCh38
NC_000006.11:g.158535859A>G , CM000668.1:g.158535859A>G	GRCh37
NC_000006.10:g.158455847A>G	NCBI36
NG_032889.1:g.58454T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.858T>C	ENSP00000391168.2:n.858T>C
ENST00000607071.6:c.*1366T>C	ENSP00000475855.1:n.*1366T>C
ENST00000642244.1:c.1556T>C	ENSP00000493554.1:p.Leu519Pro
ENST00000642903.1:c.1646T>C	ENSP00000493559.1:p.Leu549Pro
ENST00000644972.1:c.1646T>C	ENSP00000496451.1:p.Leu549Pro
ENST00000645077.1:c.*1267T>C	ENSP00000496113.1:n.*1267T>C
ENST00000645172.1:c.*1348T>C	ENSP00000495367.1:n.*1348T>C
ENST00000646190.1:n.2977T>C
ENST00000646208.1:c.1382T>C	ENSP00000493723.1:p.Leu461Pro
ENST00000646410.1:c.1517T>C	ENSP00000494205.1:p.Leu506Pro
ENST00000646562.1:c.*1480T>C	ENSP00000496087.1:n.*1480T>C
ENST00000647468.2:c.1646T>C MANE Select	ENSP00000496731.1:p.Leu549Pro
ENST00000648111.1:c.*1334T>C	ENSP00000497275.1:n.*1334T>C
ENST00000367101.5:c.*94T>C	ENSP00000356068.1:n.*94T>C
ENST00000367104.7:c.1646T>C	ENSP00000356071.3:p.Leu549Pro
ENST00000435180.5:c.371T>C	ENSP00000391168.1:p.Leu124Pro
ENST00000606965.5:c.*207T>C	ENSP00000475808.1:n.*207T>C
ENST00000607071.5:c.*1580T>C	ENSP00000475855.1:n.*1580T>C
ENST00000607742.5:c.*2924T>C	ENSP00000475523.1:n.*2924T>C
NM_032861.3:c.1646T>C	NP_116250.3:p.Leu549Pro
NR_073096.1:n.1579T>C
XM_006715586.1:c.1436T>C	XP_006715649.1:p.Leu479Pro
XM_011536196.1:c.1625T>C	XP_011534498.1:p.Leu542Pro
XM_011536197.1:c.1532T>C	XP_011534499.1:p.Leu511Pro
XM_011536198.1:c.1436T>C	XP_011534500.1:p.Leu479Pro
XM_006715586.3:c.1436T>C	XP_006715649.1:p.Leu479Pro
XM_011536196.3:c.1625T>C	XP_011534498.1:p.Leu542Pro
XM_011536198.3:c.1436T>C	XP_011534500.1:p.Leu479Pro
XM_024446573.1:c.1646T>C	XP_024302341.1:p.Leu549Pro
XR_001743697.2:n.1677T>C
XR_942606.2:n.1728T>C
NM_032861.4:c.1646T>C MANE Select	NP_116250.3:p.Leu549Pro
NR_073096.2:n.1561T>C