Canonical Allele Identifier: CA366255122

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114902-G-A
• MyVariant Identifiers: chr6:g.158535934G>A (hg19) ; chr6:g.158114902G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114902G>A , CM000668.2:g.158114902G>A	GRCh38
NC_000006.11:g.158535934G>A , CM000668.1:g.158535934G>A	GRCh37
NC_000006.10:g.158455922G>A	NCBI36
NG_032889.1:g.58379C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.783C>T	ENSP00000391168.2:n.783C>T
ENST00000607071.6:c.*1291C>T	ENSP00000475855.1:n.*1291C>T
ENST00000642244.1:c.1481C>T	ENSP00000493554.1:p.Thr494Ile
ENST00000642903.1:c.1571C>T	ENSP00000493559.1:p.Thr524Ile
ENST00000644972.1:c.1571C>T	ENSP00000496451.1:p.Thr524Ile
ENST00000645077.1:c.*1192C>T	ENSP00000496113.1:n.*1192C>T
ENST00000645172.1:c.*1273C>T	ENSP00000495367.1:n.*1273C>T
ENST00000646190.1:n.2902C>T
ENST00000646208.1:c.1307C>T	ENSP00000493723.1:p.Thr436Ile
ENST00000646410.1:c.1442C>T	ENSP00000494205.1:p.Thr481Ile
ENST00000646562.1:c.*1405C>T	ENSP00000496087.1:n.*1405C>T
ENST00000647468.2:c.1571C>T MANE Select	ENSP00000496731.1:p.Thr524Ile
ENST00000648111.1:c.*1259C>T	ENSP00000497275.1:n.*1259C>T
ENST00000367101.5:c.*19C>T	ENSP00000356068.1:n.*19C>T
ENST00000367104.7:c.1571C>T	ENSP00000356071.3:p.Thr524Ile
ENST00000435180.5:c.296C>T	ENSP00000391168.1:p.Thr99Ile
ENST00000606965.5:c.*132C>T	ENSP00000475808.1:n.*132C>T
ENST00000607071.5:c.*1505C>T	ENSP00000475855.1:n.*1505C>T
ENST00000607742.5:c.*2849C>T	ENSP00000475523.1:n.*2849C>T
NM_032861.3:c.1571C>T	NP_116250.3:p.Thr524Ile
NR_073096.1:n.1504C>T
XM_006715586.1:c.1361C>T	XP_006715649.1:p.Thr454Ile
XM_011536196.1:c.1550C>T	XP_011534498.1:p.Thr517Ile
XM_011536197.1:c.1457C>T	XP_011534499.1:p.Thr486Ile
XM_011536198.1:c.1361C>T	XP_011534500.1:p.Thr454Ile
XM_006715586.3:c.1361C>T	XP_006715649.1:p.Thr454Ile
XM_011536196.3:c.1550C>T	XP_011534498.1:p.Thr517Ile
XM_011536198.3:c.1361C>T	XP_011534500.1:p.Thr454Ile
XM_024446573.1:c.1571C>T	XP_024302341.1:p.Thr524Ile
XR_001743697.2:n.1602C>T
XR_942606.2:n.1653C>T
NM_032861.4:c.1571C>T MANE Select	NP_116250.3:p.Thr524Ile
NR_073096.2:n.1486C>T