Canonical Allele Identifier: CA406313935

Gene: BCAM

Linked Data

• MyVariant Identifiers: chr19:g.45315486A>T (hg19) ; chr19:g.44812229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44812229A>T , CM000681.2:g.44812229A>T	GRCh38
NC_000019.9:g.45315486A>T , CM000681.1:g.45315486A>T	GRCh37
NC_000019.8:g.50007326A>T	NCBI36
NG_007480.1:g.8149A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000270233.12:c.271A>T MANE Select	ENSP00000270233.5:p.Thr91Ser
ENST00000591520.6:c.208A>T	ENSP00000467100.2:p.Thr70Ser
ENST00000611077.5:c.271A>T	ENSP00000481153.1:p.Thr91Ser
ENST00000270233.10:c.271A>T	ENSP00000270233.5:p.Thr91Ser
ENST00000588603.1:n.266A>T
ENST00000589651.5:c.271A>T	ENSP00000476710.1:p.Thr91Ser
ENST00000591520.5:c.208A>T	ENSP00000467100.1:p.Thr70Ser
ENST00000611077.4:c.271A>T	ENSP00000481153.1:p.Thr91Ser
NM_001013257.2:c.271A>T	NP_001013275.1:p.Thr91Ser
NM_005581.4:c.271A>T	NP_005572.2:p.Thr91Ser
NM_005581.5:c.271A>T MANE Select	NP_005572.2:p.Thr91Ser