Canonical Allele Identifier: CA1619318300
Gene: HSPA1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31815431A= , CM000668.2:g.31815431A= GRCh38
NC_000006.11:g.31783208A= , CM000668.1:g.31783208A= GRCh37
NC_000006.10:g.31891187A= NCBI36
NG_011855.1:g.4628T=

Transcript Alleles

HGVS Amino-acid Change
XM_005249071.1:c.-14+19T= XP_005249128.1:n.-14+19T=
XM_005249073.2:c.-13-3446T= XP_005249130.1:n.-13-3446T=
XM_011514566.1:c.-13-3446T= XP_011512868.1:n.-13-3446T=