Canonical Allele Identifier: CA366255191

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535961G>A (hg19) ; chr6:g.158114929G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114929G>A , CM000668.2:g.158114929G>A	GRCh38
NC_000006.11:g.158535961G>A , CM000668.1:g.158535961G>A	GRCh37
NC_000006.10:g.158455949G>A	NCBI36
NG_032889.1:g.58352C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.756C>T	ENSP00000391168.2:n.756C>T
ENST00000607071.6:c.*1264C>T	ENSP00000475855.1:n.*1264C>T
ENST00000642244.1:c.1454C>T	ENSP00000493554.1:p.Pro485Leu
ENST00000642903.1:c.1544C>T	ENSP00000493559.1:p.Pro515Leu
ENST00000644972.1:c.1544C>T	ENSP00000496451.1:p.Pro515Leu
ENST00000645077.1:c.*1165C>T	ENSP00000496113.1:n.*1165C>T
ENST00000645172.1:c.*1246C>T	ENSP00000495367.1:n.*1246C>T
ENST00000646190.1:n.2875C>T
ENST00000646208.1:c.1280C>T	ENSP00000493723.1:p.Pro427Leu
ENST00000646410.1:c.1415C>T	ENSP00000494205.1:p.Pro472Leu
ENST00000646562.1:c.*1378C>T	ENSP00000496087.1:n.*1378C>T
ENST00000647468.2:c.1544C>T MANE Select	ENSP00000496731.1:p.Pro515Leu
ENST00000648111.1:c.*1232C>T	ENSP00000497275.1:n.*1232C>T
ENST00000367101.5:c.1588C>T	ENSP00000356068.1:p.Gln530Ter
ENST00000367104.7:c.1544C>T	ENSP00000356071.3:p.Pro515Leu
ENST00000435180.5:c.269C>T	ENSP00000391168.1:p.Pro90Leu
ENST00000606965.5:c.*105C>T	ENSP00000475808.1:n.*105C>T
ENST00000607071.5:c.*1478C>T	ENSP00000475855.1:n.*1478C>T
ENST00000607742.5:c.*2822C>T	ENSP00000475523.1:n.*2822C>T
NM_032861.3:c.1544C>T	NP_116250.3:p.Pro515Leu
NR_073096.1:n.1477C>T
XM_006715586.1:c.1334C>T	XP_006715649.1:p.Pro445Leu
XM_011536196.1:c.1523C>T	XP_011534498.1:p.Pro508Leu
XM_011536197.1:c.1430C>T	XP_011534499.1:p.Pro477Leu
XM_011536198.1:c.1334C>T	XP_011534500.1:p.Pro445Leu
XM_006715586.3:c.1334C>T	XP_006715649.1:p.Pro445Leu
XM_011536196.3:c.1523C>T	XP_011534498.1:p.Pro508Leu
XM_011536198.3:c.1334C>T	XP_011534500.1:p.Pro445Leu
XM_024446573.1:c.1544C>T	XP_024302341.1:p.Pro515Leu
XR_001743697.2:n.1575C>T
XR_942606.2:n.1626C>T
NM_032861.4:c.1544C>T MANE Select	NP_116250.3:p.Pro515Leu
NR_073096.2:n.1459C>T